Autoimmune Dementia: Predictors of Neuronal Synaptic Antibodies in Patients With New-ONset Cognitive Impairment and Their Relevance in Non-encephalitic formS: The ADONIS Study

Status: Recruiting
Location: See all (3) locations...
Study Type: Observational
SUMMARY

The goal of this observational study is to investigate the frequency and the possible pathogenic role of neuronal synaptic antibodies (NSAb) in patients with cognitive impairment (CI). The main questions it aims to answer are: 1. the frequency and associated features of NSAb in patients with CI and the usefulness of a clinical score in improving autoimmune dementia (AID) diagnosis; 2. the clinical significance of NSAb in patients with CI not fulfilling the autoimmune encephalitis (AE) criteria and serum NSAb (NSAb-pos-CI); 3. the impact of blood-brain-barrier (BBB) dysfunction on their pathogenicity.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Maximum Age: 90
View:

• both sexes

• adult (aged between 40 and 90 years)

• patients with a diagnosis of new-onset neurocognitive disorders (major and minor), as defined by the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria, with onset within the previous 24 months

Locations
Other Locations
Italy
IRCCS Istituto delle Scienze Neurologiche di Bologna
RECRUITING
Bologna
Fondazione IRCCS Istituto Neurologico Carlo Besta
RECRUITING
Milan
Istituto Auxologico Italiano IRCCS
RECRUITING
Milan
Contact Information
Primary
Maria Pia Giannoccaro, Dr.
mariapia.giannoccaro@ausl.bologna.it
+390514966112
Time Frame
Start Date: 2023-05-10
Estimated Completion Date: 2026-06-30
Participants
Target number of participants: 300
Treatments
retrospective cohort
patients with a diagnosis of new-onset neurocognitive disorders (major and minor) with onset within the previous 24 months
prospective cohort
patients with a diagnosis of new-onset neurocognitive disorders (major and minor) with onset within the previous 24 months
Related Therapeutic Areas
Sponsors
Leads: Azienda Usl di Bologna

This content was sourced from clinicaltrials.gov